75% DISINFECTANT ALCOHOL liquid

75% Disinfectant Alcohol by

Drug Labeling and Warnings

75% Disinfectant Alcohol by is a Otc medication manufactured, distributed, or labeled by CANNAPRESSO HEALTH. INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75%

Purpose

It has killing effect on Escherichia coli, Staphylococcus aureus, Candida albicans and natural bacteria (common bacteria in hospital infection).

Use

1. Human skin disinfection: Dip a cotton swab or cotton ball ( or spray) with an appropriate amount of disinfectant, and wipe the area to be treated 1-2 times for 1.5 minutes
2. Disinfect the surface of the object: use a cotton swab or cotton ball (or spray) to wipe the surface of the object with an appropriate amount of disinfectant for 1.5 minutes.

Warnings

1. This product is a disinfectant for external use and should not be taken orally.
2. Please place it out of reach of children.
3. This product is flammable and away from fire sources.
4. Use with caution in alcohol allergies.
5. After opening the product, it should be sealed in time to avoid volatilization

Do not use

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WHEN USING

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STOP USE

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KEEP OUT OF REACH OF CHILDREN

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Directions

1. This product is a disinfectant for external use and should not be taken orally.
2. Please place it out of reach of children.
3. This product is flammable and away from fire sources.
4. Use with caution in alcohol allergies.
5. After opening the product, it should be sealed in time to avoid volatilization

Other information

Inactive ingredients

Water 25%

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

75% DISINFECTANT ALCOHOL 
75% disinfectant alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75242-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75242-008-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
2	NDC: 75242-008-02	99 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
3	NDC: 75242-008-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
4	NDC: 75242-008-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
5	NDC: 75242-008-05	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
6	NDC: 75242-008-06	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
7	NDC: 75242-008-07	499 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020
8	NDC: 75242-008-08	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/21/2020

Labeler - CANNAPRESSO HEALTH. INC (117477763)

Establishment
Name	Address	ID/FEI	Business Operations
CANNAPRESSO HEALTH. INC		117477763	manufacture(75242-008)